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Diseases
Genes (972)
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MED12
Fg Syndrome
Phyllodes Tumor
POLG
Merrf Syndrome
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
WRN
Werner Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
Phyllodes Tumor
SLC2A10
Arterial Tortuosity Syndrome
SLC2A1
Arterial Tortuosity Syndrome
Adenoid Cystic Carcinoma
Glut1 Deficiency
Werner Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
GALE
Galactose Epimerase Deficiency
TP53
Adenoid Cystic Carcinoma
Werner Syndrome
Phyllodes Tumor
TRNL1
Merrf Syndrome
SETD2
Adenoid Cystic Carcinoma
Phyllodes Tumor
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
LIPA
Acid Lipase Disease
CD55
Protein Losing Enteropathy
Human Parainfluenza Viruses